DE1793813A1 - Verfahren zur herstellung von ashydrindacen und 1-(4'-as-hydrindacenyl)3-phenylpropan - Google Patents
Verfahren zur herstellung von ashydrindacen und 1-(4'-as-hydrindacenyl)3-phenylpropanInfo
- Publication number
 - DE1793813A1 DE1793813A1 DE19651793813 DE1793813A DE1793813A1 DE 1793813 A1 DE1793813 A1 DE 1793813A1 DE 19651793813 DE19651793813 DE 19651793813 DE 1793813 A DE1793813 A DE 1793813A DE 1793813 A1 DE1793813 A1 DE 1793813A1
 - Authority
 - DE
 - Germany
 - Prior art keywords
 - reaction
 - indane
 - phenylpropane
 - hydrindacenyl
 - hydrindacene
 - Prior art date
 - Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
 - Pending
 
Links
- 238000000034 method Methods 0.000 title claims description 7
 - 230000008569 process Effects 0.000 title claims description 4
 - 238000002360 preparation method Methods 0.000 title description 5
 - ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical compound CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 title description 3
 - PQNFLJBBNBOBRQ-UHFFFAOYSA-N indane Chemical compound C1=CC=C2CCCC2=C1 PQNFLJBBNBOBRQ-UHFFFAOYSA-N 0.000 claims description 78
 - 238000006243 chemical reaction Methods 0.000 claims description 37
 - WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 claims description 12
 - 239000007788 liquid Substances 0.000 claims description 7
 - 229910015900 BF3 Inorganic materials 0.000 claims description 6
 - KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 4
 - ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 4
 - 229910000040 hydrogen fluoride Inorganic materials 0.000 claims description 4
 - 238000004519 manufacturing process Methods 0.000 claims description 3
 - 239000007858 starting material Substances 0.000 claims description 3
 - 239000001294 propane Substances 0.000 claims description 2
 - 239000007795 chemical reaction product Substances 0.000 description 10
 - NUHSROFQTUXZQQ-UHFFFAOYSA-N isopentenyl diphosphate Chemical compound CC(=C)CCO[P@](O)(=O)OP(O)(O)=O NUHSROFQTUXZQQ-UHFFFAOYSA-N 0.000 description 9
 - 230000035484 reaction time Effects 0.000 description 9
 - 238000013459 approach Methods 0.000 description 8
 - 239000012044 organic layer Substances 0.000 description 7
 - 239000007791 liquid phase Substances 0.000 description 6
 - 239000001257 hydrogen Substances 0.000 description 5
 - 229910052739 hydrogen Inorganic materials 0.000 description 5
 - IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
 - VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 4
 - 238000009835 boiling Methods 0.000 description 4
 - 239000000047 product Substances 0.000 description 4
 - 230000004044 response Effects 0.000 description 4
 - UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
 - UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
 - 238000010521 absorption reaction Methods 0.000 description 3
 - 239000003054 catalyst Substances 0.000 description 3
 - 238000004587 chromatography analysis Methods 0.000 description 3
 - 238000006317 isomerization reaction Methods 0.000 description 3
 - 239000010410 layer Substances 0.000 description 3
 - -1 monosubstituted benzene Chemical class 0.000 description 3
 - VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
 - 239000000126 substance Substances 0.000 description 3
 - IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
 - UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
 - 239000002253 acid Substances 0.000 description 2
 - 239000011260 aqueous acid Substances 0.000 description 2
 - 125000003118 aryl group Chemical group 0.000 description 2
 - 230000015572 biosynthetic process Effects 0.000 description 2
 - 230000000052 comparative effect Effects 0.000 description 2
 - 150000001875 compounds Chemical class 0.000 description 2
 - 238000010438 heat treatment Methods 0.000 description 2
 - 229930195733 hydrocarbon Natural products 0.000 description 2
 - 150000002430 hydrocarbons Chemical class 0.000 description 2
 - 229910052757 nitrogen Inorganic materials 0.000 description 2
 - 239000012071 phase Substances 0.000 description 2
 - 230000008707 rearrangement Effects 0.000 description 2
 - 238000001228 spectrum Methods 0.000 description 2
 - XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
 - PJDWNSYGMXODTB-UHFFFAOYSA-N 1,2,3,4,4a,4b,5,6-octahydrophenanthrene Chemical compound C1=CCCC2C(CCCC3)C3=CC=C21 PJDWNSYGMXODTB-UHFFFAOYSA-N 0.000 description 1
 - VTIBBOHXBURHMD-UHFFFAOYSA-N 1,2,3,4,4a,5,10,10a-octahydroanthracene Chemical compound C1=CCC2CC(CCCC3)C3=CC2=C1 VTIBBOHXBURHMD-UHFFFAOYSA-N 0.000 description 1
 - ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
 - VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
 - 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
 - 238000005481 NMR spectroscopy Methods 0.000 description 1
 - 239000003463 adsorbent Substances 0.000 description 1
 - XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
 - 229910052782 aluminium Inorganic materials 0.000 description 1
 - 238000004458 analytical method Methods 0.000 description 1
 - 229910052796 boron Inorganic materials 0.000 description 1
 - 125000004432 carbon atom Chemical group C* 0.000 description 1
 - 238000013375 chromatographic separation Methods 0.000 description 1
 - 238000003776 cleavage reaction Methods 0.000 description 1
 - 238000001816 cooling Methods 0.000 description 1
 - 230000000694 effects Effects 0.000 description 1
 - 238000010828 elution Methods 0.000 description 1
 - 239000007789 gas Substances 0.000 description 1
 - 239000001307 helium Substances 0.000 description 1
 - 229910052734 helium Inorganic materials 0.000 description 1
 - SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
 - 150000002431 hydrogen Chemical class 0.000 description 1
 - 239000005457 ice water Substances 0.000 description 1
 - 239000012442 inert solvent Substances 0.000 description 1
 - 238000002329 infrared spectrum Methods 0.000 description 1
 - 239000002917 insecticide Substances 0.000 description 1
 - 238000002844 melting Methods 0.000 description 1
 - 230000008018 melting Effects 0.000 description 1
 - 238000002156 mixing Methods 0.000 description 1
 - 239000000203 mixture Substances 0.000 description 1
 - 230000004048 modification Effects 0.000 description 1
 - 238000012986 modification Methods 0.000 description 1
 - 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
 - 238000003822 preparative gas chromatography Methods 0.000 description 1
 - 229920002379 silicone rubber Polymers 0.000 description 1
 - 239000004945 silicone rubber Substances 0.000 description 1
 - 238000003756 stirring Methods 0.000 description 1
 - 238000003860 storage Methods 0.000 description 1
 - 238000006277 sulfonation reaction Methods 0.000 description 1
 - CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
 - 230000009466 transformation Effects 0.000 description 1
 - 238000005292 vacuum distillation Methods 0.000 description 1
 - 239000000080 wetting agent Substances 0.000 description 1
 
Classifications
- 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C13/00—Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
 - C07C13/28—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
 - C07C13/32—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings
 - C07C13/54—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with three condensed rings
 - C07C13/573—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with three condensed rings with three six-membered rings
 - C07C13/58—Completely or partially hydrogenated anthracenes
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C13/00—Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
 - C07C13/28—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
 - C07C13/32—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings
 - C07C13/54—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with three condensed rings
 - C07C13/547—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with three condensed rings at least one ring not being six-membered, the other rings being at the most six-membered
 - C07C13/553—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with three condensed rings at least one ring not being six-membered, the other rings being at the most six-membered with an indacene or hydrogenated indacene ring system
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C13/00—Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
 - C07C13/28—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
 - C07C13/32—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings
 - C07C13/54—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with three condensed rings
 - C07C13/573—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with three condensed rings with three six-membered rings
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
 - C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
 - C07C2/04—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
 - C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
 - C07C5/27—Rearrangement of carbon atoms in the hydrocarbon skeleton
 - C07C5/2702—Catalytic processes not covered by C07C5/2732 - C07C5/31; Catalytic processes covered by both C07C5/2732 and C07C5/277 simultaneously
 - C07C5/271—Catalytic processes not covered by C07C5/2732 - C07C5/31; Catalytic processes covered by both C07C5/2732 and C07C5/277 simultaneously with inorganic acids; with salts or anhydrides of acids
 - C07C5/2718—Acids of halogen; Salts thereof; complexes thereof with organic compounds
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C6/00—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
 - C07C6/08—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond
 - C07C6/10—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond in hydrocarbons containing no six-membered aromatic rings
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C6/00—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
 - C07C6/08—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond
 - C07C6/12—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond of exclusively hydrocarbons containing a six-membered aromatic ring
 - C07C6/123—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond of exclusively hydrocarbons containing a six-membered aromatic ring of only one hydrocarbon
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
 - C07C2527/06—Halogens; Compounds thereof
 - C07C2527/08—Halides
 - C07C2527/10—Chlorides
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
 - C07C2527/06—Halogens; Compounds thereof
 - C07C2527/08—Halides
 - C07C2527/12—Fluorides
 - C07C2527/1206—Hydrogen fluoride
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
 - C07C2527/06—Halogens; Compounds thereof
 - C07C2527/08—Halides
 - C07C2527/12—Fluorides
 - C07C2527/1213—Boron fluoride
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C2602/00—Systems containing two condensed rings
 - C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
 - C07C2602/04—One of the condensed rings being a six-membered aromatic ring
 - C07C2602/08—One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C2603/00—Systems containing at least three condensed rings
 - C07C2603/02—Ortho- or ortho- and peri-condensed systems
 - C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
 - C07C2603/06—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
 - C07C2603/10—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C2603/00—Systems containing at least three condensed rings
 - C07C2603/02—Ortho- or ortho- and peri-condensed systems
 - C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
 - C07C2603/22—Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
 - C07C2603/24—Anthracenes; Hydrogenated anthracenes
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C2603/00—Systems containing at least three condensed rings
 - C07C2603/02—Ortho- or ortho- and peri-condensed systems
 - C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
 - C07C2603/22—Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
 - C07C2603/26—Phenanthrenes; Hydrogenated phenanthrenes
 
 
Landscapes
- Chemical & Material Sciences (AREA)
 - Organic Chemistry (AREA)
 - Chemical Kinetics & Catalysis (AREA)
 - Inorganic Chemistry (AREA)
 - Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
 - Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
 
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| US34768564A | 1964-02-27 | 1964-02-27 | |
| US38869364A | 1964-08-10 | 1964-08-10 | |
| US534428A US3336407A (en) | 1964-02-27 | 1966-03-15 | Catalytic conversion of 1, 2, 3, 4-tetrahydronaphthalene, indan, and other materials | 
Publications (1)
| Publication Number | Publication Date | 
|---|---|
| DE1793813A1 true DE1793813A1 (de) | 1976-07-01 | 
Family
ID=27407791
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| DE19651793813 Pending DE1793813A1 (de) | 1964-02-27 | 1965-02-26 | Verfahren zur herstellung von ashydrindacen und 1-(4'-as-hydrindacenyl)3-phenylpropan | 
| DE19671618864 Pending DE1618864A1 (de) | 1964-02-27 | 1967-03-15 | Verfahren zur katalytischen Umwandlung von Tetralin,Indan und anderen Materialien | 
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| DE19671618864 Pending DE1618864A1 (de) | 1964-02-27 | 1967-03-15 | Verfahren zur katalytischen Umwandlung von Tetralin,Indan und anderen Materialien | 
Country Status (11)
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| GB1116052A (en) * | 1966-04-21 | 1968-06-06 | British Iron Steel Research | Improvements in and relating to the analysis of molten materials | 
| US3412166A (en) * | 1966-09-20 | 1968-11-19 | Sun Oil Co | Conversion of hydrocarbons containing the nucleus of 1, 2, 3, 4-tetrahydronaphthalene to hydrocarbons containing the nucleus of indene | 
| US3453342A (en) * | 1967-12-14 | 1969-07-01 | Sun Oil Co | Method of making 9-methyloctahydroanthracene and 9-methyloctahydro phenanthrene | 
| US3534114A (en) * | 1968-03-26 | 1970-10-13 | Sun Oil Co | Combination of gd alumino-silicate catalyst and hydrogenation catalyst | 
| US4458047A (en) * | 1982-06-07 | 1984-07-03 | Sun Tech, Inc. | Process for making naphthalene hydrodimer mixtures, product mixtures made thereby and their use as a plasticizer | 
| JPS601354B2 (ja) * | 1982-10-14 | 1985-01-14 | 出光興産株式会社 | トラクシヨンドライブ用流体 | 
| US5087785A (en) * | 1990-12-03 | 1992-02-11 | Union Camp Corporation | Processes for preparing alkylated indanes and tetrahydronaphthalenes | 
| CA2109541A1 (en) * | 1992-12-04 | 1994-06-05 | Thomas J. Ford | Aromatic oil and process for manufacture | 
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| BE503246A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1950-05-15 | |||
| US2884469A (en) * | 1956-03-26 | 1959-04-28 | Standard Oil Co | Upgrading fused benzenoid ring hydrocarbons | 
| US3197518A (en) * | 1962-04-04 | 1965-07-27 | Ashland Oil Inc | Interconversion of hydrocarbon ring compounds | 
| US3244758A (en) * | 1963-03-20 | 1966-04-05 | Sun Oil Co | Reaction of aromatic hydrocarbons with diolefins | 
- 
        0
        
- BE BE660353D patent/BE660353A/xx unknown
 
 - 
        1965
        
- 1965-02-02 GB GB4517/63A patent/GB1024500A/en not_active Expired
 - 1965-02-16 FI FI0370/65A patent/FI42827B/fi active
 - 1965-02-19 NO NO156854A patent/NO121779B/no unknown
 - 1965-02-23 SE SE02338/65A patent/SE350250B/xx unknown
 - 1965-02-25 CH CH949069A patent/CH499476A/de not_active IP Right Cessation
 - 1965-02-25 CH CH264665A patent/CH477381A/de not_active IP Right Cessation
 - 1965-02-26 NL NL656502502A patent/NL144256B/xx unknown
 - 1965-02-26 DE DE19651793813 patent/DE1793813A1/de active Pending
 - 1965-02-27 DK DK103665AA patent/DK120590B/da unknown
 
 - 
        1966
        
- 1966-03-15 US US534428A patent/US3336407A/en not_active Expired - Lifetime
 - 1966-09-12 DK DK469866AA patent/DK112445B/da unknown
 
 - 
        1967
        
- 1967-02-21 NL NL6702589A patent/NL6702589A/xx unknown
 - 1967-03-08 CH CH340867A patent/CH519449A/de not_active IP Right Cessation
 - 1967-03-15 BE BE695546D patent/BE695546A/xx unknown
 - 1967-03-15 GB GB02144/67A patent/GB1178735A/en not_active Expired
 - 1967-03-15 FR FR98842A patent/FR92718E/fr not_active Expired
 - 1967-03-15 DE DE19671618864 patent/DE1618864A1/de active Pending
 
 - 
        1969
        
- 1969-09-17 FI FI2659/69A patent/FI42829B/fi active
 - 1969-10-15 NO NO4111/69A patent/NO121894B/no unknown
 
 
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